Scleromyxedema without monoclonal gammopathy
Scleromyxedema without monoclonal gammopathy is a form of atypical lichen myxedematosus (see this term) characterized by a generalized sclerodermoid infiltration of skin studded with multiple firm papules of 1-3 mm in diameter involving face (leonine appearance) trunk and limbs without monoclonal gammopathy. The involvement of the face can be missing and pruritus may be prominent.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Scleromyxedema without monoclonal gammopathy?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Clinical Trials
For a list of clinical trials in this disease area, please click here.